Canonical Allele Identifier: CA2495826359
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403034G= , CM000664.2:g.47403034G= GRCh38
NC_000002.11:g.47630173G= , CM000664.1:g.47630173G= GRCh37
NC_000002.10:g.47483677G= NCBI36
NG_007110.2:g.4911G= , LRG_218:g.4911G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-158G= ENSP00000233146.2:n.-158G=